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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725862Generated: November 1, 2026

p-Toluenesulfonic acid monohydrate → HCID 54589357, compound

https://huagongshe.com/reaction/1725862

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantCalcium ChlorideHCID 5284359—
ReactantEthyl 2-(6-fluoro-1-hydroxy-1-indanyl)acetateHCID 23293626—
SolventTolueneHCID 1140—
ProductHCID 54589357HCID 5458935721.4%

Reaction Steps

The crude (6-Fluoro-1-hydroxy-indan-1-yl)-acetic acid ethyl ester (Compound G in FIG. 7; 3.55 g), p-toluene sulfonic acid•H2O (PTSA; 5.67 g, 29.8 mmol), and CaCl2 (4.13 g, 37.2 mmol) in toluene (66 mL) were refluxed overnight. The solution was filtered and the solid residue washed with benzene. The combined organics were washed with water, NaHCO3, water, dried (MgSO4), filtered, and concentrated in vacuo. Purification using flash chromatography (13:1 hexane/EtOAc) afforded the title compound (Compound H in FIG. 7) as an orange solid (0.703 g). 1H NMR (CDCl3) δ 7.25 (m, 2H), 7.06 (m, 1H), 6.25 (d, J=2.3 Hz, 1H), 4.24 (q, J=7.0 Hz, 2H), 3.32 (s, 2H), 3.03 (s, 2H), 1.33 (t, J=7.1 Hz, 3H); ESI-CID 221 (M-H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491744B2
Source datasetuspto-grants-2009_02
ORD IDord-09492884d2e147b38388e9db07daca1d
Source noteuspto-grants-2009_02